FDA Inspection 874728 — Keurig Dr Pepper Inc.

Keurig Dr Pepper Inc. — FEI 3024786768

The FDA completed an inspection of Keurig Dr Pepper Inc. on April 11, 2014 in Frisco, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 11, 2014
Fiscal Year
2014
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Frisco, TX (United States)